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Graphene oxide disruption of homeostasis and regeneration processes in freshwater planarian Dugesia japonica via intracellular redox deviation and apoptosis

The aquatic system is a major sink for engineered nanomaterials released into the environment. Here, we assessed the toxicity of graphene oxide (GO) using the freshwater planarian Dugesia japonica, an invertebrate model that has been widely used for studying the effects of toxins on tissue regenerat...

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Published in:Ecotoxicology and environmental safety 2023-01, Vol.249, p.114431, Article 114431
Main Authors: Xie, Changjian, Li, Xiaowei, Guo, Zhiling, Dong, Yuling, Zhang, Shujing, Li, Ao, Ma, Shan, Xu, Jianing, Pang, Qiuxiang, Peijnenburg, Willie J.G.M., Lynch, Iseult, Zhang, Peng
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cited_by cdi_FETCH-LOGICAL-c474t-bfb23a5454d63b5faa7177b9f2db2be00709b606250e56c76dcb498112da94143
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container_start_page 114431
container_title Ecotoxicology and environmental safety
container_volume 249
creator Xie, Changjian
Li, Xiaowei
Guo, Zhiling
Dong, Yuling
Zhang, Shujing
Li, Ao
Ma, Shan
Xu, Jianing
Pang, Qiuxiang
Peijnenburg, Willie J.G.M.
Lynch, Iseult
Zhang, Peng
description The aquatic system is a major sink for engineered nanomaterials released into the environment. Here, we assessed the toxicity of graphene oxide (GO) using the freshwater planarian Dugesia japonica, an invertebrate model that has been widely used for studying the effects of toxins on tissue regeneration and neuronal development. GO not only impaired the growth of normal (homeostatic) worms, but also inhibited the regeneration processes of regenerating (amputated) worms, with LC10 values of 9.86 mg/L and 9.32 mg/L for the 48-h acute toxicity test, respectively. High concentration (200 mg/L) of GO killed all the worms after 3 (regenerating) or 4 (homeostasis) days of exposure. Whole-mount in situ hybridization (WISH) and immunofluorescence analyses suggest GO impaired stem cell proliferation and differentiation, and subsequently caused cell apoptosis and oxidative DNA damage during planarian regeneration. Mechanistic analysis suggests that GO disturbed the antioxidative system (enzymatic and non-enzymatic) and energy metabolism in the planarian at both molecular and genetic levels, thus causing reactive oxygen species (ROS) over accumulation and oxidative damage, including oxidative DNA damage, loss of mitochondrial membrane integrity, lack of energy supply for cell differentiation and proliferation leading to retardance of neuron regeneration. The intrinsic oxidative potential of GO contributes to the GO-induced toxicity in planarians. These data suggest that GO in aquatic systems can cause oxidative stress and neurotoxicity in planarians. Overall, regenerated tissues are more sensitive to GO toxicity than homeostatic ones, suggesting that careful handling and appropriate decisions are needed in the application of GO to achieve healing and tissue regeneration. [Display omitted] •This is the first report of GO induced toxicity in Dugesia japonica planarian.•Low dose of GO impaired behavior and regeneration of freshwater planarian.•The intrinsic oxidative potential of GO contributes to the toxicity in planarian.•GO disrupts the antioxidative system and energy metabolism in planarian.
doi_str_mv 10.1016/j.ecoenv.2022.114431
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Here, we assessed the toxicity of graphene oxide (GO) using the freshwater planarian Dugesia japonica, an invertebrate model that has been widely used for studying the effects of toxins on tissue regeneration and neuronal development. GO not only impaired the growth of normal (homeostatic) worms, but also inhibited the regeneration processes of regenerating (amputated) worms, with LC10 values of 9.86 mg/L and 9.32 mg/L for the 48-h acute toxicity test, respectively. High concentration (200 mg/L) of GO killed all the worms after 3 (regenerating) or 4 (homeostasis) days of exposure. Whole-mount in situ hybridization (WISH) and immunofluorescence analyses suggest GO impaired stem cell proliferation and differentiation, and subsequently caused cell apoptosis and oxidative DNA damage during planarian regeneration. Mechanistic analysis suggests that GO disturbed the antioxidative system (enzymatic and non-enzymatic) and energy metabolism in the planarian at both molecular and genetic levels, thus causing reactive oxygen species (ROS) over accumulation and oxidative damage, including oxidative DNA damage, loss of mitochondrial membrane integrity, lack of energy supply for cell differentiation and proliferation leading to retardance of neuron regeneration. The intrinsic oxidative potential of GO contributes to the GO-induced toxicity in planarians. These data suggest that GO in aquatic systems can cause oxidative stress and neurotoxicity in planarians. Overall, regenerated tissues are more sensitive to GO toxicity than homeostatic ones, suggesting that careful handling and appropriate decisions are needed in the application of GO to achieve healing and tissue regeneration. [Display omitted] •This is the first report of GO induced toxicity in Dugesia japonica planarian.•Low dose of GO impaired behavior and regeneration of freshwater planarian.•The intrinsic oxidative potential of GO contributes to the toxicity in planarian.•GO disrupts the antioxidative system and energy metabolism in planarian.</description><identifier>ISSN: 0147-6513</identifier><identifier>EISSN: 1090-2414</identifier><identifier>DOI: 10.1016/j.ecoenv.2022.114431</identifier><identifier>PMID: 36521269</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Development toxicity ; Graphene oxide ; Oxidative stress ; Planarian ; Regeneration ; Stem cell</subject><ispartof>Ecotoxicology and environmental safety, 2023-01, Vol.249, p.114431, Article 114431</ispartof><rights>2023 The Authors</rights><rights>Copyright © 2022. 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Mechanistic analysis suggests that GO disturbed the antioxidative system (enzymatic and non-enzymatic) and energy metabolism in the planarian at both molecular and genetic levels, thus causing reactive oxygen species (ROS) over accumulation and oxidative damage, including oxidative DNA damage, loss of mitochondrial membrane integrity, lack of energy supply for cell differentiation and proliferation leading to retardance of neuron regeneration. The intrinsic oxidative potential of GO contributes to the GO-induced toxicity in planarians. These data suggest that GO in aquatic systems can cause oxidative stress and neurotoxicity in planarians. Overall, regenerated tissues are more sensitive to GO toxicity than homeostatic ones, suggesting that careful handling and appropriate decisions are needed in the application of GO to achieve healing and tissue regeneration. [Display omitted] •This is the first report of GO induced toxicity in Dugesia japonica planarian.•Low dose of GO impaired behavior and regeneration of freshwater planarian.•The intrinsic oxidative potential of GO contributes to the toxicity in planarian.•GO disrupts the antioxidative system and energy metabolism in planarian.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>36521269</pmid><doi>10.1016/j.ecoenv.2022.114431</doi><orcidid>https://orcid.org/0000-0002-1573-7924</orcidid><oa>free_for_read</oa></addata></record>
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1090-2414
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source Elsevier; Elsevier ScienceDirect Journals
subjects Development toxicity
Graphene oxide
Oxidative stress
Planarian
Regeneration
Stem cell
title Graphene oxide disruption of homeostasis and regeneration processes in freshwater planarian Dugesia japonica via intracellular redox deviation and apoptosis
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